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Pulmonary Fibrosis in Children

Identifieur interne : 000503 ( Main/Exploration ); précédent : 000502; suivant : 000504

Pulmonary Fibrosis in Children

Auteurs : Nadia Nathan [France] ; Chiara Sileo [France] ; Guillaume Thouvenin [France] ; Laura Berdah [France] ; Céline Delestrain [France] ; Effrosyne Manali [Grèce] ; Spyros Papiris [Grèce] ; Pierre-Louis Léger [France] ; Hubert Ducou Le Pointe [France] ; Aurore Coulomb L Ermine [France] ; Annick Clement [France]

Source :

RBID : PMC:6780823

Abstract

Pulmonary fibrosis (PF) is a very rare condition in children, which may be observed in specific forms of interstitial lung disease. None of the clinical, radiological, or histological descriptions used for PF diagnosis in adult patients, especially in situations of idiopathic PF, can apply to pediatric situations. This observation supports the view that PF expression may differ with age and, most likely, may cover distinct entities. The present review aims at summarizing the current understanding of PF pathophysiology in children and identifying suitable diagnostic criteria.


Url:
DOI: 10.3390/jcm8091312
PubMed: 31455000
PubMed Central: 6780823


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<p>Pulmonary fibrosis (PF) is a very rare condition in children, which may be observed in specific forms of interstitial lung disease. None of the clinical, radiological, or histological descriptions used for PF diagnosis in adult patients, especially in situations of idiopathic PF, can apply to pediatric situations. This observation supports the view that PF expression may differ with age and, most likely, may cover distinct entities. The present review aims at summarizing the current understanding of PF pathophysiology in children and identifying suitable diagnostic criteria.</p>
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